Canonical Allele Identifier: CA241233834
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs3832846
gnomAD v2: 12-91505304-A-AGG
gnomAD v3: 12-91111527-A-AGG
gnomAD v4: 12-91111527-A-AGG
COSMIC: COSN20109952 COSN20109953 COSN20109954 COSN20109955 COSN20109956 COSN20109957
MyVariant Identifiers: chr12:g.91505310_91505311insGG (hg19) chr12:g.91505309_91505310insGG (hg19) chr12:g.91505305_91505306insGG (hg19) chr12:g.91505304_91505305insGG (hg19) chr12:g.91111533_91111534insGG (hg38) chr12:g.91111532_91111533insGG (hg38) chr12:g.91111528_91111529insGG (hg38) chr12:g.91111527_91111528insGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111532_91111533dup , CM000674.2:g.91111532_91111533dup GRCh38
NC_000012.11:g.91505309_91505310dup , CM000674.1:g.91505309_91505310dup GRCh37
NC_000012.10:g.90029440_90029441dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-153_-152dup ENSP00000266718.4:n.-153_-152dup
NM_002345.3:c.-153_-152dup NP_002336.1:n.-153_-152dup
Search 100 bp 5'
Search 100 bp 3'